Ophthalmology, Lund
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- 1997
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Mark
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
- Contribution to journal › Article
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Mark
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267–Leu
- Contribution to journal › Article
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Mark
Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135–Trp): Disease phenotype in a Swedish family
- Contribution to journal › Article
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Mark
Pre-eclampsia is a potent risk factor for deterioration of retinopathy during pregnancy in Type 1 diabetic patients
- Contribution to journal › Article
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Mark
Poor metabolic control, early age at onset, and marginal folate deficiency are associated with increasing levels of plasma homocysteine in insulin-dependent diabetes mellitus. A five-year follow-up study
- Contribution to journal › Article
-
Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
(1997)
- Thesis › Doctoral thesis (compilation)
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Mark
Laurence-Moon-Bardet-Biedl syndrome. Clinical,electrophysiological and genetic aspects.
(1997)
- Thesis › Doctoral thesis (compilation)
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Mark
Effects of glial cell line-derived neurotrophic factor on axonal growth and apoptosis in adult mammalian sensory neurons in vitro
- Contribution to journal › Article
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Mark
Immunocytochemical localisation of neuronal nitric oxide synthase in developing and transplanted rabbit retinas
- Contribution to journal › Article
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Mark
DNA fragmentation characteristic of apoptosis and cell loss induced by kainic acid in rabbit retinas
- Contribution to journal › Article
